Division of HIV Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, USA.
J Infect Dis. 2024 Nov 15;230(5):1271-1278. doi: 10.1093/infdis/jiae180.
Flu-like reactions can occur after exposure to rifampin, rifapentine, or isoniazid. Prior studies have reported the presence of antibodies to rifampin, but associations with underlying pathogenesis are unclear.
We evaluated PREVENT TB study participants who received weekly isoniazid plus rifapentine for 3 months (3HP) or daily isoniazid for 9 months (9H) as treatment for Mycobacterium tuberculosis infection. Flu-like reaction was defined as a grade ≥2 of any of flu-like symptoms. Controls (3HP or 9H) did not report flu-like reactions. We developed a competitive enzyme-linked immunosorbent assays (ELISA) to detect antibodies against rifapentine, isoniazid, rifampin, and rifapentine metabolite.
Among 128 participants, 69 received 3HP (22 with flu-like reactions; 47 controls) and 59 received 9H (12 with flu-like reactions; 47 controls). In participants receiving 3HP, anti-rifapentine IgG was identified in 2 of 22 (9%) participants with flu-like reactions and 6 of 47 (13%) controls (P = .7), anti-isoniazid IgG in 2 of 22 (9%) participants with flu-like reactions and 4 of 47 (9%) controls (P = .9). Among participants receiving 9H, IgG and IgM anti-isoniazid antibodies were each present in 4 of 47 (9%) controls, but none among participants with flu-like reactions; anti-rifapentine IgG antibodies were not present in any participants with flu-like reactions or controls.
We detected anti-rifapentine, anti-isoniazid, and anti-rifapentine metabolite antibodies, but the proportions of participants with antibodies were low, and did not differ between participants with flu-like reactions and those without such reactions. This suggests that flu-like reactions associated with 3HP and 9H were not antibody mediated.
NCT00023452.
利福平、利福喷丁或异烟肼暴露后可发生流感样反应。先前的研究报告了针对利福平的抗体的存在,但与潜在发病机制的关联尚不清楚。
我们评估了接受每周异烟肼加利福喷丁治疗 3 个月(3HP)或每日异烟肼治疗 9 个月(9H)治疗结核分枝杆菌感染的 PREVENT TB 研究参与者。流感样反应定义为任何流感样症状的等级≥2。对照(3HP 或 9H)未报告流感样反应。我们开发了竞争性酶联免疫吸附试验(ELISA)来检测针对利福喷丁、异烟肼、利福平及利福喷丁代谢物的抗体。
在 128 名参与者中,69 名接受 3HP(22 名有流感样反应;47 名对照),59 名接受 9H(12 名有流感样反应;47 名对照)。在接受 3HP 的参与者中,22 名有流感样反应的参与者中有 2 名(9%)和 47 名对照中有 6 名(13%)检测到抗利福喷丁 IgG(P=0.7),22 名有流感样反应的参与者中有 2 名(9%)和 47 名对照中有 4 名(9%)检测到抗异烟肼 IgG(P=0.9)。在接受 9H 的参与者中,47 名对照中有 4 名(9%)分别存在 IgG 和 IgM 抗异烟肼抗体,但在有流感样反应的参与者中均未发现;有流感样反应的参与者和对照中均未发现抗利福喷丁 IgG 抗体。
我们检测到抗利福喷丁、抗异烟肼和抗利福喷丁代谢物抗体,但参与者抗体的比例较低,且在有流感样反应的参与者和无流感样反应的参与者之间无差异。这表明与 3HP 和 9H 相关的流感样反应不是抗体介导的。
NCT00023452。